LIFESHIELD LATEX-FREE MICROBORE EXTENSION SET, MODEL 14949 AND OTHERS— 510(k) K052722

Unknown

Hospira, Inc.

FDA 510(k) clearance K052722 for LIFESHIELD LATEX-FREE MICROBORE EXTENSION SET, MODEL 14949 AND OTHERS, Unknown on 2005-11-02. Applicant: Hospira, Inc..

Clearance details

Applicant: Hospira, Inc.
Product code: Code FPA
Advisory panel: General Hospital
Date received: 2005-09-29
Decision date: 2005-11-02
Decision: Unknown
Clearance type: Special
Location: Lake Forest, IL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FPA

product code FPA

Death: 95
Injury: 14,421
Malfunction: 125,815
Other: 30
Total: 140,361

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.